Canonical Allele Identifier: CA346463132

Gene: ALK

Linked Data

• MyVariant Identifiers: chr2:g.29445246T>G (hg19) ; chr2:g.29222380T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29222380T>G , CM000664.2:g.29222380T>G	GRCh38
NC_000002.11:g.29445246T>G , CM000664.1:g.29445246T>G	GRCh37
NC_000002.10:g.29298750T>G	NCBI36
NG_009445.1:g.704187A>C , LRG_488:g.704187A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3479A>C MANE Select	ENSP00000373700.3:p.Asp1160Ala
ENST00000431873.6:c.706A>C
ENST00000638605.1:n.356A>C
ENST00000642122.1:c.275A>C	ENSP00000493203.1:p.Asp92Ala
ENST00000389048.7:c.3479A>C	ENSP00000373700.3:p.Asp1160Ala
ENST00000431873.5:c.359A>C	ENSP00000414027.2:p.Asp120Ala
ENST00000453137.1:c.173A>C	ENSP00000387488.1:p.Asp58Ala
ENST00000618119.4:c.2348A>C	ENSP00000482733.1:p.Asp783Ala
NM_004304.4:c.3479A>C	NP_004295.2:p.Asp1160Ala
NM_001353765.1:c.275A>C	NP_001340694.1:p.Asp92Ala
XM_024452778.1:c.632A>C	XP_024308546.1:p.Asp211Ala
XM_024452779.1:c.275A>C	XP_024308547.1:p.Asp92Ala
NM_004304.5:c.3479A>C MANE Select	NP_004295.2:p.Asp1160Ala
NM_001353765.2:c.275A>C	NP_001340694.1:p.Asp92Ala